Asymmetric total synthesis and structural elucidation of NFAT-68.

Asymmetric total synthesis and structural elucidation of NFAT-68.
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NFAT-68 的不对称全合成和结构解析。

DOI:
10.1021/ol102574d
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发表时间:
2011
期刊:
影响因子:
5.2
通讯作者:
Zhen Yang
Zhen Yang
中科院分区:
化学1区
文献类型:
--
作者:
Lin Wang;Yumeng Xi;Shouliang Yang;R. Zhu;Yufan Liang;Jia;Zhen Yang

文献摘要

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完成了NFAT-68(7)的全合成,并测定了其相对立体化学。其关键步骤是利用螯合控制的乙烯基向山羟醛缩合反应(VMAR)立体选择性地合成顺式羟醛产物8。这一化学方法的发展有望在许多其他天然产物的全合成中得到更广泛的应用。
Total synthesis of NFAT-68 (7) has been achieved and its relative stereochemistry has been determined. A key step thereof is the utilization of the chelation-controlled vinylogous Mukaiyama aldol reaction (VMAR) to stereoselectively synthesize the syn-aldol product 8. This developed chemistry is anticipated to have wider application in total syntheses of many other natural products.